Triflic Anhydride-Mediated Cycloacylation of [60]Fullerene with 1-Naphthoic Acids: Synthesis and Derivatization of [60]Fullerene-Fused Dihydrophenalenones

An efficient triflic anhydride-mediated synthesis of [60]fullerene (C<sub>60</sub>)-fused dihydrophenalenones from C<sub>60</sub> and 1-naphthoic acids has been developed, representing the first one-step construction of C<sub>60</sub>-fused polyaromatic ketones under metal-free conditions. In addition, the C<sub>60</sub>-fused dihydrophenalenones can be reduced to C<sub>60</sub>-fused dihydrophenalenes and C<sub>60</sub>-fused dihydrophenalenols. The structures of the products were unambiguously established by single-crystal X-ray diffraction. A possible reaction mechanism is proposed based on control experiments. Furthermore, a representative C<sub>60</sub>-fused dihydrophenalenone was employed as a third component in organic solar cells, leading to improved device performance.

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Publication Details

Journal
Organic Letters
Published
2026-03-16
DOI
https://doi.org/10.1021/acs.orglett.6c00679
Primary Topic
Fullerene Chemistry and Applications
Type
article
Field-Weighted Citation Impact
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article

Triflic Anhydride-Mediated Cycloacylation of [60]Fullerene with 1-Naphthoic Acids: Synthesis and Derivatization of [60]Fullerene-Fused Dihydrophenalenones

Chong Niu, Zheng‐Chun Yin, Wen-Jie Qiu, Xinmin Huang et al.
Organic Letters
Fullerene Chemistry and Applications
article

Triflic Anhydride-Mediated Cycloacylation of [60]Fullerene with 1-Naphthoic Acids: Synthesis and Derivatization of [60]Fullerene-Fused Dihydrophenalenones

Chong Niu, Zheng‐Chun Yin, Wen-Jie Qiu, Xinmin Huang, Zhiwei Xu, Guan-Wu Wang
article en

Abstract

An efficient triflic anhydride-mediated synthesis of [60]fullerene (C<sub>60</sub>)-fused dihydrophenalenones from C<sub>60</sub> and 1-naphthoic acids has been developed, representing the first one-step construction of C<sub>60</sub>-fused polyaromatic ketones under metal-free conditions. In addition, the C<sub>60</sub>-fused dihydrophenalenones can be reduced to C<sub>60</sub>-fused dihydrophenalenes and C<sub>60</sub>-fused dihydrophenalenols. The structures of the products were unambiguously established by single-crystal X-ray diffraction. A possible reaction mechanism is proposed based on control experiments. Furthermore, a representative C<sub>60</sub>-fused dihydrophenalenone was employed as a third component in organic solar cells, leading to improved device performance.

Organic LettersVol. 28(12)
University of Science and Technology of China (CN), State Key Laboratory of Chemical Engineering (CN), Anhui Normal University (CN), Lanzhou University (CN)
Affordable and clean energy
Openalex Percentile: Top 19%
Fullerene Chemistry and Applications
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